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"46708-567-90" National Drug Code (NDC)
Erlotinib Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (46708-567-90)
(Alembic Pharmaceuticals Limited)
NDC Code
46708-567-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (46708-567-90)
Product NDC
46708-567
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib Hydrochloride
Non-Proprietary Name
Erlotinib Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210709
Marketing Category Name
ANDA
Application Number
ANDA214719
Manufacturer
Alembic Pharmaceuticals Limited
Substance Name
ERLOTINIB HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/46708-567-90